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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71011Generated: October 26, 2026

Acetonitrile → Benzathine

https://huagongshe.com/reaction/71011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantAtorvastatinHCID 60823—
SolventWaterHCID 962—
ProductBenzathineHCID 8793—
ProductAtorvastatinHCID 60823—
Product3-Phenylpropane-1,2-diamineHCID 413434—

Reaction Steps

The benzathine salt of atorvastatin (Form B) was synthesized by preparing a stock solution of the free acid of atorvastatin (U.S. Pat. No. 5,273,995) in acetonitrile (1 g in 40 mL of ACN). A solution of N,N′-bis(phenylmethyl-1,2-ethanediamine (benzathine) was prepared by dissolving 220.64 mg (0.5 equivalents) in acetonitrile (80 mL) and water (20 mL). The stock solution of atorvastatin free acid was added to the counterion solution with stirring. After 2 days of stirring at ambient temperature, the solids were isolated by vacuum filtration using a Buchner funnel fitted with a paper filter (#2 Whatman). The solids were rinsed with acetonitrile (75 mL) to afford atorvastatin benzathine Form B. Note that this procedure is the same as above except that the sample was not oven dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822703B2
Source datasetuspto-grants-2014_09
ORD IDord-45777a62c3a540f0aec199c98e0a898a
Source noteuspto-grants-2014_09